Gene-specific Copy Number Variation Probe-HADHB
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| Catalog: |
CNVFP-HADHB-06358 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (HADHB). The product usually consists of a combination of reagents, which consists of a probe with a selected dye color and a hybridization reagent. We provide CNV FISH Probes with a variety of dye color combinations to meet various challenges. Probe products not only provide some classic color combinations but also provide customized probe services. |
| Application: |
HADHB Gene-specific copy number variation probes are mainly used to detect the copy number variation related to HADHB genes. This product achieves the purpose of detection by hybridizing with the HADHB gene. Due to this design method, our probe products can detect the amplification and deletion of target genes on chromosomes through FISH. |
| Category: |
Copy Number Variation |
| Probe Kits Volume (µL): |
40 μL |
| Quantity: |
20 Tests |
| Hybridization Solution (µL): |
200 μL |
| Turnaround Time: |
7-10 Business Days |
| Shipping Time: |
1-2 Day Expedited Shipping |
| Storage Conditions: |
Store at -20℃ and avoid light; |
| Shipping Conditions: |
-20℃ |
Gene Details
| Gene Name |
Hydroxyacyl-CoA Dehydrogenase Trifunctional Multienzyme Complex Subunit Beta |
| Gene Summary [Provided by RefSeq] |
This gene encodes the beta subunit of the mitochondrial trifunctional protein, which catalyzes the last three steps of mitochondrial beta-oxidation of long chain fatty acids. The mitochondrial membrane-bound heterocomplex is composed of four alpha and four beta subunits, with the beta subunit catalyzing the 3-ketoacyl-CoA thiolase activity. The encoded protein can also bind RNA and decreases the stability of some mRNAs. The genes of the alpha and beta subunits of the mitochondrial trifunctional protein are located adjacent to each other in the human genome in a head-to-head orientation. Mutations in this gene result in trifunctional protein deficiency. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2013] |
| Gene Symbol |
HADHB |
| Location |
2p23.3 |
| Chromosome |
Chromosome2 |
| Coordinates |
This gene maps to 26467615-26513333 in GRCh37 coordinates. |
| Species |
Human |
Dye Colors:
OR
RE
GO
GR
AQ
Order Sheet
| Number |
Dye Color |
Order Name |
Absorbance Maximum |
Emission Maximum |
Add to Cart |
| 1 |
OR
|
CNVFP-HADHB-06358-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-HADHB-06358-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-HADHB-06358-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-HADHB-06358-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-HADHB-06358-AQ |
467nm |
418nm |
|
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